Product Recalls in Michigan

Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,698 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,698 in last 12 months

Showing 75617580 of 13,418 recalls

DrugSeptember 28, 2017· Leading Pharma, LLC

Recalled Item: Lorazepam Tablets Recalled by Leading Pharma, LLC Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength. Bottle labeled as 0.5 mg tablets...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2017· United Pharmacy

Recalled Item: Glutamine Recalled by United Pharmacy Due to CGMP Deviations; FDA analysis...

The Issue: CGMP Deviations; FDA analysis deterrmined that the product does not contain...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2017· The Harvard Drug Group

Recalled Item: Alprazolam Tablets Recalled by The Harvard Drug Group Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification result...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2017· Pharmedium Services, LLC

Recalled Item: Phenylephrine HCL 100 mcg per mL (1 mg/10 mL) in Recalled by Pharmedium...

The Issue: Superpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2017· Pharmedium Services, LLC

Recalled Item: morphine Sulfate in 0.9% Sodium Chloride Injection 2 mL Total Recalled by...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 26, 2017· Pharmedium Services, LLC

Recalled Item: morphine Sulfate in 0.9% Sodium Chloride Injection 1 mL Total Volume 2 mg...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 26, 2017· Pharmedium Services, LLC

Recalled Item: HYDROmorphone HCl in 0.9% Sodium Chloride Injection Recalled by Pharmedium...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2017· Sandoz Inc

Recalled Item: Ampicillin for Injection Recalled by Sandoz Inc Due to Labeling: Missing...

The Issue: Labeling: Missing Label: customer complaint that some vials of ampicillin...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2017· Precision Dose Inc.

Recalled Item: Carbamazepine Oral Suspension USP Recalled by Precision Dose Inc. Due to...

The Issue: Subpotent Drug: low out of specification results.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2017· Amneal Pharmaceuticals, Inc.

Recalled Item: Esterified Estrogens & Methyltestosterone Tablets Recalled by Amneal...

The Issue: Subpotent Drug: Out of specification assay result in Esterified Estrogen and...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2017· Amneal Pharmaceuticals, Inc.

Recalled Item: Esterified Estrogens & Methyltestosterone Tablets Recalled by Amneal...

The Issue: Subpotent Drug: Out of specification assay result in Esterified Estrogen and...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Suture Removal Tray Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Suture Removal Tray Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Abdominal Surgery II Pack-LF Recalled by Medline Industries Inc Due...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline General Purpose Tray Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline NICC Suture Removal Tray Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Skin Staple Remover Kit Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Skin Biopsy Pack-LF Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medical Equipment Affiliates IV Start Kit Recalled by Medline Industries Inc...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline General Purpose Tray Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund